Have questions? Visit https://www.reddit.com/r/SNPedia

rs111033482

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033482(A;C)
Make rs111033482(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position77189373
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033482
ebirs111033482
HLIrs111033482
Exacrs111033482
Varsomers111033482
Maprs111033482
PheGenIrs111033482
hapmaprs111033482
1000 genomesrs111033482
hgdprs111033482
ensemblrs111033482
gopubmedrs111033482
geneviewrs111033482
scholarrs111033482
googlers111033482
pharmgkbrs111033482
gwascentralrs111033482
openSNPrs111033482
23andMers111033482
23andMe allrs111033482
SNP Nexus

SNPshotrs111033482
SNPdbers111033482
MSV3drs111033482
GWAS Ctlgrs111033482
Max Magnitude0
ClinVar
Risk rs111033482(C;C)
Alt rs111033482(C;C)
Reference rs111033482(A;A)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76900418A>C
CLNSRC ClinVar
CLNACC RCV000036114.2,